BN Business News
Add your company to Business Communicator →

Business · 15/02/1995

FDA Proposes New Requirements for Implanted Urinary Continence Devices

The FDA is proposing to require premarket approval for a medical device used to treat urinary incontinence, citing potential risks and benefits, and invites public input on a potential classification change.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

Explore insights